Protein-protein interactions

ABSTRACT

The present invention relates to the discovery of novel protein-protein interactions that are involved in mammalian physiological pathways, including physiological disorders or diseases. Examples of physiological disorders and diseases include non-insulin dependent diabetes mellitus (NIDDM), neurodegenerative disorders, such as Alzheimer&#39;s Disease (AD), and the like. Thus, the present invention is directed to complexes of these proteins and/or their fragments, antibodies to the complexes, diagnosis of physiological generative disorders (including diagnosis of a predisposition to and diagnosis of the existence of the disorder), drug screening for agents which modulate the interaction of proteins described herein, and identification of additional proteins in the pathway common to the proteins described herein.

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] The present application is related to U.S. provisional patent application Serial No. 60/259,572, filed on Jan. 4, 2001, incorporated herein by reference, and claims priority thereto under 35 USC §119(e).

BACKGROUND OF THE INVENTION

[0002] The present invention relates to the discovery of novel protein-protein interactions that are involved in mammalian physiological pathways, including physiological disorders or diseases. Examples of physiological disorders and diseases include non-insulin dependent diabetes mellitus (NIDDM), neurodegenerative disorders, such as Alzheimer's Disease (AD), and the like. Thus, the present invention is directed to complexes of these proteins and/or their fragments, antibodies to the complexes, diagnosis of physiological generative disorders (including diagnosis of a predisposition to and diagnosis of the existence of the disorder), drug screening for agents which modulate the interaction of proteins described herein, and identification of additional proteins in the pathway common to the proteins described herein.

[0003] The publications and other materials used herein to illuminate the background of the invention, and in particular, cases to provide additional details respecting the practice, are incorporated herein by reference, and for convenience, are referenced by author and date in the following text and respectively grouped in the appended Bibliography.

[0004] Many processes in biology, including transcription, translation and metabolic or signal transduction pathways, are mediated by non-covalently associated protein complexes. The formation of protein-protein complexes or protein-DNA complexes produce the most efficient chemical machinery. Much of modern biological research is concerned with identifying proteins involved in cellular processes, determining their functions, and how, when and where they interact with other proteins involved in specific pathways. Further, with rapid advances in genome sequencing, there is a need to define protein linkage maps, i.e., detailed inventories of protein interactions that make up functional assemblies of proteins or protein complexes or that make up physiological pathways.

[0005] Recent advances in human genomics research has led to rapid progress in the identification of novel genes. In applications to biological and pharmaceutical research, there is a need to determine functions of gene products. A first step in defining the function of a novel gene is to determine its interactions with other gene products in appropriate context. That is, since proteins make specific interactions with other proteins or other biopolymers as part of functional assemblies or physiological pathways, an appropriate way to examine function of a gene is to determine its physical relationship with other genes. Several systems exist for identifying protein interactions and hence relationships between genes.

[0006] There continues to be a need in the art for the discovery of additional protein-protein interactions involved in mammalian physiological pathways. There continues to be a need in the art also to identify the protein-protein interactions that are involved in mammalian physiological disorders and diseases, and to thus identify drug targets.

SUMMARY OF THE INVENTION

[0007] The present invention relates to the discovery of protein-protein interactions that are involved in mammalian physiological pathways, including physiological disorders or diseases, and to the use of this discovery. The identification of the interacting proteins described herein provide new targets for the identification of useful pharmaceuticals, new targets for diagnostic tools in the identification of individuals at risk, sequences for production of transformed cell lines, cellular models and animal models, and new bases for therapeutic intervention in such physiological pathways

[0008] Thus, one aspect of the present invention is protein complexes. The protein complexes are a complex of (a) two interacting proteins, (b) a first interacting protein and a fragment of a second interacting protein, (c) a fragment of a first interacting protein and a second interacting protein, or (d) a fragment of a first interacting protein and a fragment of a second interacting protein. The fragments of the interacting proteins include those parts of the proteins, which interact to form a complex. This aspect of the invention includes the detection of protein interactions and the production of proteins by recombinant techniques. The latter embodiment also includes cloned sequences, vectors, transfected or transformed host cells and transgenic animals.

[0009] A second aspect of the present invention is an antibody that is immunoreactive with the above complex. The antibody may be a polyclonal antibody or a monoclonal antibody. While the antibody is immunoreactive with the complex, it is not immunoreactive with the component parts of the complex. That is, the antibody is not immunoreactive with a first interactive protein, a fragment of a first interacting protein, a second interacting protein or a fragment of a second interacting protein. Such antibodies can be used to detect the presence or absence of the protein complexes.

[0010] A third aspect of the present invention is a method for diagnosing a predisposition for physiological disorders or diseases in a human or other animal. The diagnosis of such disorders includes a diagnosis of a predisposition to the disorders and a diagnosis for the existence of the disorders. In accordance with this method, the ability of a first interacting protein or fragment thereof to form a complex with a second interacting protein or a fragment thereof is assayed, or the genes encoding interacting proteins are screened for mutations in interacting portions of the protein molecules. The inability of a first interacting protein or fragment thereof to form a complex, or the presence of mutations in a gene within the interacting domain, is indicative of a predisposition to, or existence of a disorder. In accordance with one embodiment of the invention, the ability to form a complex is assayed in a two-hybrid assay. In a first aspect of this embodiment, the ability to form a complex is assayed by a yeast two-hybrid assay. In a second aspect, the ability to form a complex is assayed by a mammalian two-hybrid assay. In a second embodiment, the ability to form a complex is assayed by measuring in vitro a complex formed by combining said first protein and said second protein. In one aspect the proteins are isolated from a human or other animal. In a third embodiment, the ability to form a complex is assayed by measuring the binding of an antibody, which is specific for the complex. In a fourth embodiment, the ability to form a complex is assayed by measuring the binding of an antibody that is specific for the complex with a tissue extract from a human or other animal. In a fifth embodiment, coding sequences of the interacting proteins described herein are screened for mutations.

[0011] A fourth aspect of the present invention is a method for screening for drug candidates which are capable of modulating the interaction of a first interacting protein and a second interacting protein. In this method, the amount of the complex formed in the presence of a drug is compared with the amount of the complex formed in the absence of the drug. If the amount of complex formed in the presence of the drug is greater than or less than the amount of complex formed in the absence of the drug, the drug is a candidate for modulating the interaction of the first and second interacting proteins. The drug promotes the interaction if the complex formed in the presence of the drug is greater and inhibits (or disrupts) the interaction if the complex formed in the presence of the drug is less. The drug may affect the interaction directly, i.e., by modulating the binding of the two proteins, or indirectly, e.g., by modulating the expression of one or both of the proteins.

[0012] A fifth aspect of the present invention is a model for such physiological pathways, disorders or diseases. The model may be a cellular model or an animal model, as further described herein. In accordance with one embodiment of the invention, an animal model is prepared by creating transgenic or “knock-out” animals. The knock-out may be a total knock-out, i.e., the desired gene is deleted, or a conditional knock-out, i.e., the gene is active until it is knocked out at a determined time. In a second embodiment, a cell line is derived from such animals for use as a model. In a third embodiment, an animal model is prepared in which the biological activity of a protein complex of the present invention has been altered. In one aspect, the biological activity is altered by disrupting the formation of the protein complex, such as by the binding of an antibody or small molecule to one of the proteins which prevents the formation of the protein complex. In a second aspect, the biological activity of a protein complex is altered by disrupting the action of the complex, such as by the binding of an antibody or small molecule to the protein complex which interferes with the action of the protein complex as described herein. In a fourth embodiment, a cell model is prepared by altering the genome of the cells in a cell line. In one aspect, the genome of the cells is modified to produce at least one protein complex described herein. In a second aspect, the genome of the cells is modified to eliminate at least one protein of the protein complexes described herein.

[0013] A sixth aspect of the present invention are nucleic acids coding for novel proteins discovered in accordance with the present invention and the corresponding proteins and antibodies.

[0014] A seventh aspect of the present invention is a method of screening for drug candidates useful for treating a physiological disorder. In this embodiment, drugs are screened on the basis of the association of a protein with a particular physiological disorder. This association is established in accordance with the present invention by identifying a relationship of the protein with a particular physiological disorder. The drugs are screened by comparing the activity of the protein in the presence and absence of the drug. If a difference in activity is found, then the drug is a drug candidate for the physiological disorder. The activity of the protein can be assayed in vitro or in vivo using conventional techniques, including transgenic animals and cell lines of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

[0015] The present invention is the discovery of novel interactions between proteins described herein. The genes coding for some of these proteins may have been cloned previously, but their potential interaction in a physiological pathway or with a particular protein was unknown. Alternatively, the genes coding for some of these proteins have not been cloned previously and represent novel genes. These proteins are identified using the yeast two-hybrid method and searching a human total brain library, as more fully described below.

[0016] According to the present invention, new protein-protein interactions have been discovered. The discovery of these interactions has identified several protein complexes for each protein-protein interaction. The protein complexes for these interactions are set forth below in Tables 1-12, which also identifies the new protein-protein interactions of the present invention. TABLE 1 Protein Complexes IKKb/LDHM Interaction  IkappaB kinase beta (IKKb) and lactate dehydrogenase A (LDHM)  A fragment of IKKb and LDHM  IKKb and a fragment of LDHM  A fragment of IKKb and a fragment of LDHM

[0017] TABLE 2 Protein Complexes IKKb/EIF3S10 Interaction IkappaB kinase beta (IKKb) and translation initiation factor 3 (EIF3S10) A fragment of IKKb and EIF3S10 IKKb and a fragment of EIF3S10 A fragment of IKKb and a fragment of EIF3S10

[0018] TABLE 3 Protein Complexes IKKb/SLAP2 Interaction IkappaB kinase beta (IKKb) and sarcolemmal associated protein-2 (SLAP2) A fragment of IKKb and SLAP2 IKKb and a fragment of SLAP2 A fragment of IKKb and a fragment of SLAP2

[0019] TABLE 4 Protein Complexes IKKb/KIAA0614 Interaction IkappaB kinase beta (IKKb) and KIAA0614 A fragment of IKKb and KIAA0614 IKKb and a fragment of KIAA0614 A fragment of IKKb and a fragment of KIAA0614

[0020] TABLE 5 Protein Complexes IKKb/SART-1 Interaction IkappaB kinase beta (IKKb) and SART-1 A fragment of IKKb and SART-1 IKKb and a fragment of SART-1 A fragment of IKKb and a fragment of SART-1

[0021] TABLE 6 Protein Complexes IKKb/GBDR1 Interaction IkappaB kinase beta (IKKb) and glialblastoma differentiation- related protein (GBDR1) A fragment of IKKb and GBDR1 IKKb and a fragment of GBDR1 A fragment of IKKb and a fragment of GBDR1

[0022] TABLE 7 Protein Complexes IKKa/GBDR1 Interaction IkappaB kinase alpha (IKKa) and glialblastoma differentiation-related protein (GBDR1) A fragment of IKKa and GBDR1 IKKa and a fragment of GBDR1 A fragment of IKKa and a fragment of GBDR1

[0023] TABLE 8 Protein Complexes IKKg/I-TRAF Interaction IkappaB kinase gamma (IKKg) and TRAF-interacting protein (I-TRAF) A fragment of IKKg and I-TRAF IKKg and a fragment of I-TRAF A fragment of IKKg and a fragment of I-TRAF

[0024] TABLE 9 Protein Complexes IKK-i/I-TRAF Interaction IkappaB kinase, inducible (IKK-i) and TRAF-interacting protein (I-TRAF) A fragment of IKK-i and I-TRAF IKK-i and a fragment of I-TRAF A fragment of IKK-i and a fragment of I-TRAF

[0025] TABLE 10 Protein Complexes IKK-i/NUMA1 Interaction IkappaB kinase, inducible (IKK-i) and nuclear mitotic apparatus protein 1 (NUMA1) A fragment of IKK-i and NUMA1 IKK-i and a fragment of NUMA1 A fragment of IKK-i and a fragment of NUMA1

[0026] TABLE 11 Protein Complexes IKK-i/SPA-1 Interaction IkappaB kinase, inducible (IKK-i) and signal-induced proliferation associated protein (SPA1) A fragment of IKK-i and SPA1 IKK-i and a fragment of SPA1 A fragment of IKK-i and a fragment of SPA1

[0027] TABLE 12 Protein Complexes IKK-i/PN13730 Interaction IkappaB kinase, inducible (IKK-i) and novel protein PN13730 A fragment of IKK-i and PN13730 IKK-i and a fragment of PN13730 A fragment of IKK-i and a fragment of PN13730

[0028] The involvement of above interactions in particular pathways is as follows.

[0029] Many cellular proteins exert their function by interacting with other proteins in the cell. Examples of this are found in the formation of multiprotein complexes and the association of enzymes with their substrates. It is widely believed that a great deal of information can be gained by understanding individual protein-protein interactions, and that this is useful in identifying complex networks of interacting proteins that participate in the workings of normal cellular functions. Ultimately, the knowledge gained by characterizing these networks can lead to valuable insight into the causes of human diseases and can eventually lead to the development of therapeutic strategies. The yeast two-hybrid assay is a powerful tool for determining protein-protein interactions and it has been successfully used for studying human disease pathways. In one variation of this technique, a protein of interest (or a portion of that protein) is expressed in a population of yeast cells that collectively contain all protein sequences. Yeast cells that possess protein sequences that interact with the protein of interest are then genetically selected, and the identity of those interacting proteins are determined by DNA sequencing. Thus, proteins that can be demonstrated to interact with a protein known to be involved in a human disease are therefore also implicated in that disease. Proteins identified in the first round of two-hybrid screening can be subsequently used in a second round of two-hybrid screening, allowing the identification of multiple proteins in the complex network of interactions in a disease pathway.

[0030] Nuclear factor kappaB (NFkB) is an inducible transcription factor that regulates a large number of genes, particularly those involved in the inflammatory and immune responses (Barnes and Karin, 1997; Baeuerle and Baichwal, 1997). NFkB has been demonstrated to be inappropriately regulated in a number of human inflammatory disorders, including rheumatoid and osteoarthritis, asthma, arteriosclerosis and inflammatory bowel disease, as well as some cancers (Luque and Gelinas, 1997; Foxwell et al., 1998; Barnes and Adcock, 1998; Neurath et al., 1998; Hatada et al., 2000). Inhibiting NFkB activation has many potential applications in treating these diseases, and consequently is an area of intense interest for drug development. One mechanism by which steroids exert their broad-spectrum anti-inflammatory action is by inhibiting the activation of NFkB. By identifying non-steroidal means of inhibiting NFkB activation, it is hoped a class of novel immunosuppressive drugs that has the potency of steroids without their toxicity can be developed.

[0031] NFkB activity is controlled by protein-protein interactions that alter its subcellular localization (Karin and Ben-Neriah, 2000; Karin, 1999; Mercurio and Manning, 1999). In unstimulated cells, NFkB is inactive and sequestered in the cytoplasm due to its interaction with IkappaB (IkB), which masks the NFkB nuclear localization signal. Upon stimulation, IkB is phosphorylated, which targets it for ubiquitination and proteasome-mediated degradation. Disruption of the IkB/NFkB complex frees NFkB to enter the nucleus and activate transcription of proinflammatory genes. A key step in NFkB activation is the initial phosphorylation of IkB; this is accomplished by IkB-kinase (IKK) family members, which are in turn responsive to signals from cell surface receptors for factors such as TNF-alpha and IL-1. Clearly, identifying all of the proteins involved in NFkB activation is necessary to understand the process by which extracellular signals are transduced into NFkB-mediated transcriptional responses. Furthermore, identification of these proteins will increase the repertoire of potential targets for therapeutic intervention in the treatment of diseases due to defects involving NFkB activation, such as arthritis, asthma, and cancer.

[0032] IkB kinases (IKKs) are responsible for signal-induced phosphorylation IkB, leading to IkB degradation and activation of NFkB. These proteins appear to function as a complex of IKK family members, and may interact with other cellular factors as well. Consequently, the IKKs and proteins with which they interact are potential targets of anti-inflammatory (and other) drugs. Four IKKs [IKK-alpha (IKKa), IKK-beta (IKKb), IKK-gamma (IKKg), and inducible IKK (IKK-i)] have been identified (reviewed in Karin and Ben-Neriah, 2000; Karin, 1999; Mercurio and Manning, 19998-10). These proteins were used in yeast two-hybrid assays to identify IKK-interacting proteins.

[0033] Six new interactions were identified for IKK-beta (IKKb). The first is with the squamous cell carcinoma antigen SART-1. SART-1 was identified as an antigen on human squamous cell carcinoma cells that is recognized by cytotoxic T-lymphocytes. SART-1 does not have any recognizable structural domains that might give clues to its function. Interestingly, SART-1 has a high degree of homology to the mouse Haf protein (GenBank accession AF129931). Haf is described as a hypoxia associated factor that induces the expression of erythropoietin and VEGF. This similarity and the interaction with IKKb suggest SART-1 is involved in intracellular signaling both in response to, and leading to the production of, cell signaling factors.

[0034] The second IKKb interactor is a subunit of translation initiation factor 3 (EIF3S10). EIF3S10 is the largest subunit of the EIF3 complex. It contains a so-called PCI domain that is found in other proteins also found in large complexes, such as components of the COP9 signalosome (Scholler et al., 1997). The interaction of EIF3S20 with IKKb suggests that phosphorylation of the translation machinery may be part of the inflammatory response. This possibility is further supported by our identification of interactions between MAPKAP-K3, a protein kinase involved in the inflammatory response, and the translation-associated proteins ERF-2, SUI1, and PAIP1.

[0035] The next IKKb interactor is the lactate dehydrogenase M chain (also known as LDH-A) was found to be an interactor. LDH is the last enzyme involved in anaerobic glycolysis, and resides in the cytosol. Although the significance of this interaction is not entirely clear, the demonstrated interaction with IKKb suggests that LDH can act as a phosphorylation substrate of IKKb, and further suggests a link between NFkB activation and cellular metabolism.

[0036] IKKb is shown to interact with the sarcolemmal-associated protein SLAP-2. The SLAP proteins are a family of amphipathic alpha-helical proteins that associate with the membrane and form coiled-coil structures (Wigle et al., 1997). We have previously identified an interaction between SLAP-2 and the insulin-regulated aminopeptidase IRAP, suggesting this protein functions both in insulin-dependent and inflammation-related signaling pathways.

[0037] We have identified an interaction between IKKb and the hypothetical protein KIAA0614. The function of KIAA0614 is largely unknown, however there does appear to be a putative HECT domain in the KIAA0614 protein sequence. The HECT domain is the consensus sequence found in ubiquitin transferases or so-called E3 ubiquitin ligases. IKKb contains a ubiquitin-like region that may be responsible for this interaction. In addition, KIAA0614 closely related to a protein described in the public databases as a protein phosphatase (GenBank accession AF174498). This suggests that KIAA0614 and IKKb may act together to control the phosphorylation status of cellular substrates such as IkB.

[0038] The next interactor, the glioblastoma cell differentiation-related protein GBDR1, was found in yeast two-hybrid searches using both IKK-alpha and IKK-beta. The function of GBDR1 is not known but sequence analysis indicates the presence of two ubiquitin-associated domains. Consistent with this, the IKK-beta used to isolate GBDR1 contains a ubiquitin-like domain. In contrast, the fragment of IKK-alpha that associates with GBDR1 includes a helix-loop-helix domain rather than the ubiquitin-like domain. Nonetheless, the interaction of the same domain of GBDR1 with two different IKKs strongly suggests this protein is part of the signal transduction cascade that leads to NFkB activation.

[0039] One interactor for IKK-gamma (IKKg, also known as NEMO) was identified. This protein, I-TRAF, is a known component of the NFkB activation cascade. I-TRAF is known to bind to the conserved C-terminal domain of TRAF proteins and inhibit TRAF-mediated NF-kappa-B activation (Ling and Goeddel, 2000). Phosphorylation of I-TRAF results in its dissociation from TRAF and the subsequent activation of NFkB. We and others have found that another IKK (IKK-i) is able to interact with, and phosphorylate, I-TRAF (Nomura et al., 2000). The interaction with IKK-gamma may similarly result in modification of I-TRAF. However, such a role for IKKg is likely indirect, since IKKg appears to be a non-catalytic IKK family member. This notion is consistent with the fact that the domain of IKK-i with which I-TRAF interacts is a C-terminal (non-kinase) region of the protein.

[0040] The inducible IkB kinase (IKK-i) was found to interact with three proteins. The first of these is the signal-induced proliferation associated protein SPA1. SPA-1 is over 90% identical to the murine homolog, which was originally isolated based on its inducible expression in lymphoid cells stimulated with IL-2; it was further shown that murine SPA1 hampers mitogen-induced cell cycle progression when abnormally or prematurely expressed (Hattori et al., 1995). The N-terminal domains of both the human and murine SPA1 proteins are highly homologous to the human Rap1 GTPase-activating protein (GAP). Human SPA1 exhibits GAP activity for Rap1 and Rap2, but not for Ras, Rho, or Ran (Kurachi et al., 1997). In addition to the N-terminal GTPase activating domain, human SPA1 contains predicted coiled-coil, PDZ, and transmembrane domains. Human SPA1 is localized primarily to the perinuclear region and is widely expressed, with highest expression levels in lymphoid organs. The interaction with IKK-i suggests SPA-1 is involved in NFkB activation.

[0041] IKK-i is also found to interact with the nuclear mitotic apparatus protein NUMA1. NUMA1 is found in the nucleus during interphase and is associated with isolated nuclear matrices, and specifically localizes to the spindle apparatus during mitosis in a manner that suggests it is involved in the early steps of nuclear reassembly (Lydersen and Pettijohn, 1980). Analysis of the 2101 amino acid NUMA1 protein reveals an unusually long central coiled-coil domain (>1400 amino acids). Interestingly, NUMA1 is one of a handful of proteins to which RAR-alpha can be fused in acute promyelocytic leukemia (APL). The most prevalent RAR-alpha fusion partner in APL is PML, and it has been proposed that disruption of PML organization is responsible for the APL phenotype. In rare cases of APL, the ligand- and DNA-binding domains of RAR-alpha are fused to the 5′ exons of NUMA1, resulting in a fusion protein that exists in sheet-like nuclear aggregates (Wells et al., 1997). Wells et al. further demonstrate that PML organization is normal in cells expressing the RAR-alpha/NUMA1 fusion, suggesting that interference with retinoid signaling, and not disruption of PML organization, is essential to the APL phenotype and implicating an element of the mitotic apparatus in the molecular pathogenesis of human malignancy. The interaction of NUMA1 with an IKK suggests that cellular processes, such as mitosis and nuclear assembly, are under control of the same signaling pathways that activate NFkB. In support of this, we have previously found interactions between NUMA1 and the signaling proteins MAPKAP-K3, PRAK, AKT1, and AKT2.

[0042] The final interaction for IKK-i is with the novel protein PN13730. PN13730 is a protein fragment 494 amino acids in length that contains predicted coiled-coil domains, a spectrin repeat, and regions similar to the leukemia inhibiting factor/oncostatin-M small cytokine signature and the syntaxin N-terminal motif. The prey construct isolated by ProNet encodes amino acids 203-493 of PN13730. EST analysis suggests that PN13730 is expressed in a number of tissues including breast, skin and ovary. Subsequent to the identification of PN13730, the full length sequence of this protein has been identified and, along with the cDNA sequence, is set forth in GenBank accession number AJ292348. PN13730 corresponds to the N-terminus of AJ292348.

[0043] The proteins disclosed in the present invention were found to interact with their corresponding proteins in the yeast two-hybrid system. Because of the involvement of the corresponding proteins in the physiological pathways disclosed herein, the proteins disclosed herein also participate in the same physiological pathways. Therefore, the present invention provides a list of uses of these proteins and DNA encoding these proteins for the development of diagnostic and therapeutic tools useful in the physiological pathways. This list includes, but is not limited to, the following examples.

Two-Hybrid System

[0044] The principles and methods of the yeast two-hybrid system have been described in detail elsewhere (e.g., Bartel and Fields, 1997; Bartel et al., 1993; Fields and Song, 1989; Chevray and Nathans, 1992). The following is a description of the use of this system to identify proteins that interact with a protein of interest.

[0045] The target protein is expressed in yeast as a fusion to the DNA-binding domain of the yeast Gal4p. DNA encoding the target protein or a fragment of this protein is amplified from cDNA by PCR or prepared from an available clone. The resulting DNA fragment is cloned by ligation or recombination into a DNA-binding domain vector (e.g., pGBT9, pGBT.C, pAS2-1) such that an in-frame fusion between the Gal4p and target protein sequences is created.

[0046] The target gene construct is introduced, by transformation, into a haploid yeast strain. A library of activation domain fusions (i.e., adult brain cDNA cloned into an activation domain vector) is introduced by transformation into a haploid yeast strain of the opposite mating type. The yeast strain that carries the activation domain constructs contains one or more Gal4p-responsive reporter gene(s), whose expression can be monitored. Examples of some yeast reporter strains include Y190, PJ69, and CBY14a. An aliquot of yeast carrying the target gene construct is combined with an aliquot of yeast carrying the activation domain library. The two yeast strains mate to form diploid yeast and are plated on media that selects for expression of one or more Gal4p-responsive reporter genes. Colonies that arise after incubation are selected for further characterization.

[0047] The activation domain plasmid is isolated from each colony obtained in the two-hybrid search. The sequence of the insert in this construct is obtained by the dideoxy nucleotide chain termination method. Sequence information is used to identify the gene/protein encoded by the activation domain insert via analysis of the public nucleotide and protein databases. Interaction of the activation domain fusion with the target protein is confirmed by testing for the specificity of the interaction. The activation domain construct is co-transformed into a yeast reporter strain with either the original target protein construct or a variety of other DNA-binding domain constructs. Expression of the reporter genes in the presence of the target protein but not with other test proteins indicates that the interaction is genuine.

[0048] In addition to the yeast two-hybrid system, other genetic methodologies are available for the discovery or detection of protein-protein interactions. For example, a mammalian two-hybrid system is available commercially (Clontech, Inc.) that operates on the same principle as the yeast two-hybrid system. Instead of transforming a yeast reporter strain, plasmids encoding DNA-binding and activation domain fusions are transfected along with an appropriate reporter gene (e.g., lacZ) into a mammalian tissue culture cell line. Because transcription factors such as the Saccharomyces cerevisiae Gal4p are functional in a variety of different eukaryotic cell types, it would be expected that a two-hybrid assay could be performed in virtually any cell line of eukaryotic origin (e.g., insect cells (SF9), fungal cells, worm cells, etc.). Other genetic systems for the detection of protein-protein interactions include the so-called SOS recruitment system (Aronheim et al., 1997).

Protein-protein Interactions

[0049] Protein interactions are detected in various systems including the yeast two-hybrid system, affinity chromatography, co-immunoprecipitation, subcellular fractionation and isolation of large molecular complexes. Each of these methods is well characterized and can be readily performed by one skilled in the art. See, e.g., U.S. Pat. Nos. 5,622,852 and 5,773,218, and PCT published applications No. WO 97/27296 and WO 99/65939, each of which are incorporated herein by reference.

[0050] The protein of interest can be produced in eukaryotic or prokaryotic systems. A cDNA encoding the desired protein is introduced in an appropriate expression vector and transfected in a host cell (which could be bacteria, yeast cells, insect cells, or mammalian cells). Purification of the expressed protein is achieved by conventional biochemical and immunochemical methods well known to those skilled in the art. The purified protein is then used for affinity chromatography studies: it is immobilized on a matrix and loaded on a column. Extracts from cultured cells or homogenized tissue samples are then loaded on the column in appropriate buffer, and non-binding proteins are eluted. After extensive washing, binding proteins or protein complexes are eluted using various methods such as a gradient of pH or a gradient of salt concentration. Eluted proteins can then be separated by two-dimensional gel electrophoresis, eluted from the gel, and identified by micro-sequencing. The purified proteins can also be used for affinity chromatography to purify interacting proteins disclosed herein. All of these methods are well known to those skilled in the art.

[0051] Similarly, both proteins of the complex of interest (or interacting domains thereof) can be produced in eukaryotic or prokaryotic systems. The proteins (or interacting domains) can be under control of separate promoters or can be produced as a fusion protein. The fusion protein may include a peptide linker between the proteins (or interacting domains) which, in one embodiment, serves to promote the interaction of the proteins (or interacting domains). All of these methods are also well known to those skilled in the art.

[0052] Purified proteins of interest, individually or a complex, can also be used to generate antibodies in rabbit, mouse, rat, chicken, goat, sheep, pig, guinea pig, bovine, and horse. The methods used for antibody generation and characterization are well known to those skilled in the art. Monoclonal antibodies are also generated by conventional techniques. Single chain antibodies are further produced by conventional techniques.

[0053] DNA molecules encoding proteins of interest can be inserted in the appropriate expression vector and used for transfection of eukaryotic cells such as bacteria, yeast, insect cells, or mammalian cells, following methods well known to those skilled in the art. Transfected cells expressing both proteins of interest are then lysed in appropriate conditions, one of the two proteins is immunoprecipitated using a specific antibody, and analyzed by polyacrylamide gel electrophoresis. The presence of the binding protein (co-immunoprecipitated) is detected by immunoblotting using an antibody directed against the other protein. Co-immunoprecipitation is a method well known to those skilled in the art.

[0054] Transfected eukaryotic cells or biological tissue samples can be homogenized and fractionated in appropriate conditions that will separate the different cellular components. Typically, cell lysates are run on sucrose gradients, or other materials that will separate cellular components based on size and density. Subcellular fractions are analyzed for the presence of proteins of interest with appropriate antibodies, using immunoblotting or immunoprecipitation methods. These methods are all well known to those skilled in the art.

Disruption of Protein-protein Interactions

[0055] It is conceivable that agents that disrupt protein-protein interactions can be beneficial in many physiological disorders, including, but not-limited to NIDDM, AD and others disclosed herein. Each of the methods described above for the detection of a positive protein-protein interaction can also be used to identify drugs that will disrupt said interaction. As an example, cells transfected with DNAs coding for proteins of interest can be treated with various drugs, and co-immunoprecipitations can be performed. Alternatively, a derivative of the yeast two-hybrid system, called the reverse yeast two-hybrid system (Leanna and Hannink, 1996), can be used, provided that the two proteins interact in the straight yeast two-hybrid system.

Modulation of Protein-protein Interactions

[0056] Since the interactions described herein are involved in a physiological pathway, the identification of agents which are capable of modulating the interactions will provide agents which can be used to track physiological disorder or to use lead compounds for development of therapeutic agents. An agent may modulate expression of the genes of interacting proteins, thus affecting interaction of the proteins. Alternatively, the agent may modulate the interaction of the proteins. The agent may modulate the interaction of wild-type with wild-type proteins, wild-type with mutant proteins, or mutant with mutant proteins. Agents which may be used to modulate the protein interaction include a peptide, an antibody, a nucleic acid, an antisense compound or a ribozyme. The nucleic acid may encode the antibody or the antisense compound. The peptide may be at least 4 amino acids of the sequence of either of the interacting proteins. Alternatively, the peptide may be from 4 to 30 amino acids (or from 8 to 20 amino acids) that is at least 75% identical to a contiguous span of amino acids of either of the interacting proteins. The peptide may be covalently linked to a transporter capable of increasing cellular uptake of the peptide. Examples of a suitable transporter include penetratins, l-Tat₄₉₋₅₇, d-Tat₄₉₋₅₇, retro-inverso isomers of l- or d-Tat₄₉₋₅₇, L-arginine oligomers, D- arginine oligomers, L-lysine oligomers, D-lysine oligomers, L-histine oligomers, D-histine oligomers, L-ornithine oligomers, D-ornithine oligomers, short peptide sequences derived from fibroblast growth factor, Galparan, and HSV-1 structural protein VP22, and peptoid analogs thereof. Agents can be tested using transfected host cells, cell lines, cell models or animals, such as described herein, by techniques well known to those of ordinary skill in the art, such as disclosed in U.S. Pat. Nos. 5,622,852 and 5,773,218, and PCT published application Nos. WO 97/27296 and WO 99/65939, each of which are incorporated herein by reference. The modulating effect of the agent can be tested in vivo or in vitro. Agents can be provided for testing in a phage display library or a combinatorial library. Exemplary of a method to screen agents is to measure the effect that the agent has on the formation of the protein complex.

Mutation Screening

[0057] The proteins disclosed in the present invention interact with one or more proteins known to be involved in a physiological pathway, such as in NIDDM, AD or pathways described herein. Mutations in interacting proteins could also be involved in the development of the physiological disorder, such as NIDDM, AD or disorders described herein, for example, through a modification of protein-protein interaction, or a modification of enzymatic activity, modification of receptor activity, or through an unknown mechanism. Therefore, mutations can be found by sequencing the genes for the proteins of interest in patients having the physiological disorder, such as insulin, and non-affected controls. A mutation in these genes, especially in that portion of the gene involved in protein interactions in the physiological pathway, can be used as a diagnostic tool and the mechanistic understanding the mutation provides can help develop a therapeutic tool.

Screening for At-risk Individuals

[0058] Individuals can be screened to identify those at risk by screening for mutations in the protein disclosed herein and identified as described above. Alternatively, individuals can be screened by analyzing the ability of the proteins of said individual disclosed herein to form natural complexes. Further, individuals can be screened by analyzing the levels of the complexes or individual proteins of the complexes or the mRNA encoding the protein members of the complexes. Techniques to detect the formation of complexes, including those described above, are known to those skilled in the art. Techniques and methods to detect mutations are well known to those skilled in the art. Techniques to detect the level of the complexes, proteins or mRNA are well known to those skilled in the art.

Cellular models of Physiological Disorders

[0059] A number of cellular models of many physiological disorders or diseases have been generated. The presence and the use of these models are familiar to those skilled in the art. As an example, primary cell cultures or established cell lines can be transfected with expression vectors encoding the proteins of interest, either wild-type proteins or mutant proteins. The effect of the proteins disclosed herein on parameters relevant to their particular physiological disorder or disease can be readily measured. Furthermore, these cellular systems can be used to screen drugs that will influence those parameters, and thus be potential therapeutic tools for the particular physiological disorder or disease. Alternatively, instead of transfecting the DNA encoding the protein of interest, the purified protein of interest can be added to the culture medium of the cells under examination, and the relevant parameters measured.

Animal Models

[0060] The DNA encoding the protein of interest can be used to create animals that overexpress said protein, with wild-type or mutant sequences (such animals are referred to as “transgenic”), or animals which do not express the native gene but express the gene of a second animal (referred to as “transplacement”), or animals that do not express said protein (referred to as “knock-out”). The knock-out animal may be an animal in which the gene is knocked out at a determined time. The generation of transgenic, transplacement and knock-out animals (normal and conditioned) uses methods well known to those skilled in the art.

[0061] In these animals, parameters relevant to the particular physiological disorder can be measured. These parametes may include receptor function, protein secretion in vivo or in vitro, survival rate of cultured cells, concentration of particular protein in tissue homogenates, signal transduction, behavioral analysis, protein synthesis, cell cycle regulation, transport of compounds across cell or nuclear membranes, enzyme activity, oxidative stress, production of pathological products, and the like. The measurements of biochemical and pathological parameters, and of behavioral parameters, where appropriate, are performed using methods well known to those skilled in the art. These transgenic, transplacement and knock-out animals can also be used to screen drugs that may influence the biochemical, pathological, and behavioral parameters relevant to the particular physiological disorder being studied. Cell lines can also be derived from these animals for use as cellular models of the physiological disorder, or in drug screening.

Rational Drug Design

[0062] The goal of rational drug design is to produce structural analogs of biologically active polypeptides of interest or of small molecules with which they interact (e.g., agonists, antagonists, inhibitors) in order to fashion drugs which are, for example, more active or stable forms of the polypeptide, or which, e.g., enhance or interfere with the function of a polypeptide in vivo. Several approaches for use in rational drug design include analysis of three-dimensional structure, alanine scans, molecular modeling and use of anti-id antibodies. These techniques are well known to those skilled in the art. Such techniques may include providing atomic coordinates defining a three-dimensional structure of a protein complex formed by said first polypeptide and said second polypeptide, and designing or selecting compounds capable of interfering with the interaction between a first polypeptide and a second polypeptide based on said atomic coordinates.

[0063] Following identification of a substance which modulates or affects polypeptide activity, the substance may be further investigated. Furthermore, it may be manufactured and/or used in preparation, i.e., manufacture or formulation, or a composition such as a medicament, pharmaceutical composition or drug. These may be administered to individuals.

[0064] A substance identified as a modulator of polypeptide function may be peptide or non-peptide in nature. Non-peptide “small molecules” are often preferred for many in vivo pharmaceutical uses. Accordingly, a mimetic or mimic of the substance (particularly if a peptide) may be designed for pharmaceutical use.

[0065] The designing of mimetics to a known pharmaceutically active compound is a known approach to the development of pharmaceuticals based on a “lead” compound. This approach might be desirable where the active compound is difficult or expensive to synthesize or where it is unsuitable for a particular method of administration, e.g., pure peptides are unsuitable active agents for oral compositions as they tend to be quickly degraded by proteases in the alimentary canal. Mimetic design, synthesis and testing is generally used to avoid randomly screening large numbers of molecules for a target property.

[0066] Once the pharmacophore has been found, its structure is modeled according to its physical properties, e.g., stereochemistry, bonding, size and/or charge, using data from a range of sources, e.g., spectroscopic techniques, x-ray diffraction data and NMR. Computational analysis, similarity mapping (which models the charge and/or volume of a pharmacophore, rather than the bonding between atoms) and other techniques can be used in this modeling process.

[0067] A template molecule is then selected, onto which chemical groups that mimic the pharmacophore can be grafted. The template molecule and the chemical groups grafted thereon can be conveniently selected so that the mimetic is easy to synthesize, is likely to be pharmacologically acceptable, and does not degrade in vivo, while retaining the biological activity of the lead in compound. Alternatively, where the mimetic is peptide-based, further stability can be achieved by cyclizing the peptide, increasing its rigidity. The mimetic or mimetics found by this approach can then be screened to see whether they have the target property, or to what extent it is exhibited. Further optimization or modification can then be carried out to arrive at one or more final mimetics for in vivo or clinical testing.

Diagnostic Assays

[0068] The identification of the interactions disclosed herein enables the development of diagnostic assays and kits, which can be used to determine a predisposition to or the existence of a physiological disorder. In one aspect, one of the proteins of the interaction is used to detect the presence of a “normal” second protein (i.e., normal with respect to its ability to interact with the first protein) in a cell extract or a biological fluid, and further, if desired, to detect the quantitative level of the second protein in the extract or biological fluid. The absence of the “normal” second protein would be indicative of a predisposition or existence of the physiological disorder. In a second aspect, an antibody against the protein complex is used to detect the presence and/or quantitative level of the protein complex. The absence of the protein complex would be indicative of a predisposition or existence of the physiological disorder.

Nucleic Acids and Proteins

[0069] A nucleic acid or fragment thereof has substantial identity with another if, when optimally aligned (with appropriate nucleotide insertions or deletions) with the other nucleic acid (or its complementary strand), there is nucleotide sequence identity in at least about 60% of the nucleotide bases, usually at least about 70%, more usually at least about 80%, preferably at least about 90%, more preferably at least about 95% of the nucleotide bases, and more preferably at least about 98% of the nucleotide bases. A protein or fragment thereof has substantial identity with another if, optimally aligned, there is an amino acid sequence identity of at least about 30% identity with an entire naturally-occurring protein or a portion thereof, usually at least about 70% identity, more ususally at least about 80% identity, preferably at least about 90% identity, more preferably at least about 95% identity, and most preferably at least about 98% identity.

[0070] Identity means the degree of sequence relatedness between two polypeptide or two polynucleotides sequences as determined by the identity of the match between two strings of such sequences. Identity can be readily calculated. While there exist a number of methods to measure identity between two polynucleotide or polypeptide sequences, the term “identity” is well known to skilled artisans (Computational Molecular Biology, Lesk, A. M., ed., Oxford University Press, New York, 1988; Biocomputing: Informatics and Genome Projects, Smith, D. W., ed., Academic Press, New York, 1993; Computer Analysis of Sequence Data, Part I, Griffin, A. M., and Griffin, H. G., eds., Humana Press, New Jersey, 1994; Sequence Analysis in Molecular Biology, von Heinje, G., Academic Press, 1987; and Sequence Analysis Primer, Gribskov, M. and Devereux, J., eds., M Stockton Press, New York, 1991). Methods commonly employed to determine identity between two sequences include, but are not limited to those disclosed in Guide to Huge Computers, Martin J. Bishop, ed., Academic Press, San Diego, 1994, and Carillo, H., and Lipman, D., SIAM J Applied Math. 48:1073 (1988). Preferred methods to determine identity are designed to give the largest match between the two sequences tested. Such methods are codified in computer programs. Preferred computer program methods to determine identity between two sequences include, but are not limited to, GCG (Genetics Computer Group, Madison Wis.) program package (Devereux, J., et al., Nucleic Acids Research 12(1).387 (1984)), BLASTP, BLASTN, FASTA (Altschul et al. (1990); Altschul et al. (1997)). The well-known Smith Waterman algorithm may also be used to determine identity.

[0071] Alternatively, substantial homology or similarity exists when a nucleic acid or fragment thereof will hybridize to another nucleic acid (or a complementary strand thereof) under selective hybridization conditions, to a strand, or to its complement. Selectivity of hybridization exists when hybridization which is substantially more selective than total lack of specificity occurs. Nucleic acid hybridization will be affected by such conditions as salt concentration, temperature, or organic solvents, in addition to the base composition, length of the complementary strands, and the number of nucleotide base mismatches between the hybridizing nucleic acids, as will be readily appreciated by those skilled in the art. Stringent temperature conditions will generally include temperatures in excess of 30° C., typically in excess of 37° C., and preferably in excess of 45° C. Stringent salt conditions will ordinarily be less than 1000 mM, typically less than 500 mM, and preferably less than 200 mM. However, the combination of parameters is much more important than the measure of any single parameter. See, e.g., Asubel, 1992; Wetmur and Davidson, 1968.

[0072] The terms “isolated”, “substantially pure”, and “substantially homogeneous” are used interchangeably to describe a protein or polypeptide which has been separated from components which accompany it in its natural state. A monomeric protein is substantially pure when at least about 60 to 75% of a sample exhibits a single polypeptide sequence. A substantially pure protein will typically comprise about 60 to 90% W/W of a protein sample, more usually about 95%, and preferably will be over about 99% pure. Protein purity or homogeneity may be indicated by a number of means well known in the art, such as polyacrylamide gel electrophoresis of a protein sample, followed by visualizing a single polypeptide band upon staining the gel. For certain purposes, higher resolution may be provided by using HPLC or other means well known in the art which are utilized for purification.

[0073] Large amounts of the nucleic acids of the present invention may be produced by (a) replication in a suitable host or transgenic animals or (b) chemical synthesis using techniques well known in the art. Constructs prepared for introduction into a prokaryotic or eukaryotic host may comprise a replication system recognized by the host, including the intended polynucleotide fragment encoding the desired polypeptide, and will preferably also include transcription and translational initiation regulatory sequences operably linked to the polypeptide encoding segment. Expression vectors may include, for example, an origin of replication or autonomously replicating sequence (ARS) and expression control sequences, a promoter, an enhancer and necessary processing information sites, such as ribosome-binding sites, RNA splice sites, polyadenylation sites, transcriptional terminator sequences, and mRNA stabilizing sequences. Secretion signals may also be included where appropriate which allow the protein to cross and/or lodge in cell membranes, and thus attain its functional topology, or be secreted from the cell. Such vectors may be prepared by means of standard recombinant techniques well known in the art.

[0074] The nucleic acid or protein may also be incorporated on a microarray. The preparation and use of microarrays are well known in the art. Generally, the microarray may contain the entire nucleic acid or protein, or it may contain one or more fragments of the nucleic acid or protein. Suitable nucleic acid fragments may include at least 17 nucleotides, at least 21 nucleotides, at least 30 nucleotides or at least 50 nucleotides of the nucleic acid sequence, particularly the coding sequence. Suitable protein fragments may include at least 4 amino acids, at least 8 amino acids, at least 12 amino acids, at least 15 amino acids, at least 17 amino acids or at least 20 amino acids. Thus, the present invention is also directed to such nucleic acid and protein fragments.

EXAMPLES

[0075] The present invention is further detailed in the following Examples, which are offered by way of illustration and are not intended to limit the invention in any manner. Standard techniques well known in the art or the techniques specifically described below are utilized.

Example 1 Yeast Two-Hybrid System

[0076] The principles and methods of the yeast two-hybrid systems have been described in detail (Bartel and Fields, 1997). The following is thus a description of the particular procedure that we used, which was applied to all proteins.

[0077] The cDNA encoding the bait protein was generated by PCR from brain cDNA. Gene-specific primers were synthesized with appropriate tails added at their 5′ ends to allow recombination into the vector pGBTQ. The tail for the forward primer was 5′-GCAGGAAACAGCTATGACCATACAGTCAGCGGCCGCCACC-3′ (SEQ ID NO:1) and the tail for the reverse primer was 5′-ACGGCCAGTCGCGTGGAGTGTTATGTCATGCGGCCGCTA-3′ (SEQ ID NO:2). The tailed PCR product was then introduced by recombination into the yeast expression vector pGBTQ, which is a close derivative of pGBTC (Bartel et al., 1996) in which the polylinker site has been modified to include M13 sequencing sites. The new construct was selected directly in the yeast J693 for its ability to drive tryptophane synthesis (genotype of this strain: Mat α, ade2, his3, leu2, trp1, URA3::GAL1-lacZ LYS2::GAL1-HIS3 gal4del gal80del cyhR2). In these yeast cells, the bait is produced as a C-terminal fusion protein with the DNA binding domain of the transcription factor Gal4 (amino acids 1 to 147). A total human brain (37 year-old male Caucasian) cDNA library cloned into the yeast expression vector pACT2 was purchased from Clontech (human brain MATCHMAKER cDNA, cat. #HL4004AH), transformed into the yeast strain J692 (genotype of this strain: Mat a, ade2, his3, leu2, trp1, URA3::GAL1-lacZ LYS2::GAL1-HIS3 gal4del gal80del cyhR2), and selected for the ability to drive leucine synthesis. In these yeast cells, each cDNA is expressed as a fusion protein with the transcription activation domain of the transcription factor Gal4 (amino acids 768 to 881) and a 9 amino acid hemagglutinin epitope tag. J693 cells (Mat α type) expressing the bait were then mated with J692 cells (Mat a type) expressing proteins from the brain library. The resulting diploid yeast cells expressing proteins interacting with the bait protein were selected for the ability to synthesize tryptophan, leucine, histidine, and β-galactosidase. DNA was prepared from each clone, transformed by electroporation into E. coli strain KC8 (Clontech KC8 electrocompetent cells, cat. #C2023-1), and the cells were selected on ampicillin-containing plates in the absence of either tryptophane (selection for the bait plasmid) or leucine (selection for the brain library plasmid). DNA for both plasmids was prepared and sequenced by dideoxynucleotide chain termination method. The identity of the bait cDNA insert was confirmed and the cDNA insert from the brain library plasmid was identified using BLAST program against public nucleotides and protein databases. Plasmids from the brain library (preys) were then individually transformed into yeast cells together with a plasmid driving the synthesis of lamin fused to the Gal4 DNA binding domain. Clones that gave a positive signal after β-galactosidase assay were considered false-positives and discarded. Plasmids for the remaining clones were transformed into yeast cells together with plasmid for the original bait. Clones that gave a positive signal after β-galactosidase assay were considered true positives.

Example 2 Identification of IKKb/LDHM Interaction

[0078] A yeast two-hybrid system as described in Example 1 using amino acids 301-602 of IKKb (GenBank (GB) accession no. AF031416) as bait was performed. One clone that was identified by this procedure included amino acids 9-332 of LDHM (GB accession no. U13679).

Example 3 Identification of IKK-i/PN13730 Interaction

[0079] A yeast two-hybrid system as described in Example 1 using amino acids 450-717 of IKK-i (GenBank (GB) accession no. D63485) as bait was performed. One clone that was identified by this procedure included amino acids 203-493 of PN13730. The DNA sequence and the predicted protein sequence for PN13730 are set forth in Tables 13 and 14, respectively. TABLE 13 Nucleotide Sequence of PN13730 gaaagtttcggttctgcccggcggtggacccacgagc (SEQ ID NO:3) gcgtgccaccatggagtctgaccactgctgagcagac agccaccgagggccgaaattctgagccttcctctgga cccaggcaggagacatacagacaagaaaggcaaactc accatggcctccaccaatgcagagagccagctccaga gaatcatccgagacttgcaagatgctgtgacagaact aagcaaagaatttcaggaagcaggggaacccatcacg gatgacagcaccagcttgcataaattttcttataaac ttgagtatctcctgcaatttgatcagaaagagaaggc caccctcctgggcaacaagaaggactactgggattac ttctgtgcctgcctggccaaggtgaaaggagccaatg atgggatccgctttgtcaagtctatctcagagctccg aacatccttggggaaaggaagagcatttattcgctac tccttggtgcaccagaggttggcagacaccttacagc agtgcttcatgaacaccaaagtgaccagtgactggta ctatgcaagaagcccctttctgcagccaaagctgagc tcggacattgtgggccaactctatgagctgactgagg ttcagtttgacctggcgtcgaggggctttgacttgga tgctgcctggccaacatttgccaggaggacgctgacc actggctcttctgcttacctgtggaaaccccctagcc gcagctccagcatgagcagcttggtgagcagctacct gcagactcaagagatggtgtccaactttgacctgaac agccccctaaacaacgaggcattggagggctttgatg agatgcgactagagctggaccagttggaggtgcggga gaagcagctacgggagcgcatgcagcagctggacaga gagaaccaggagctgagggcagctgtcagccagcaag gggagcaactgcagacagagagggagagggggcgcac tgcagcggaggacaacgttcgcctcacttgcttggta gctgagctccagaagcagtgggaggtcacccaggcca cccagaacactgtgaaggagctgcagacatgcctgca gggcctggagctaggagcagcagagaaggaggaggac taccacacagccctgcggcggctggagtccatgctgc agcccttggcacaggagcttgaggccacacgggactc actggacaagaaaaaccagcatttagccagcttccca ggctggctagccatggctcagcagaaggcagatacgg catcagacacaaagggccggcaagaacctattcccag tgatgcggcccaggagatgcaggagctaggggagaag cttcaagccctagaaagggagagaaccaaggtcgagg aggtcaacagacagcagagtgcccaactggaacagct ggtcaaggagcttcagctgaaagaggatgcccgggcc agcctggagcgcctggtgaaggagatggccccactcc aggaggagttgtctgggaagggacaggaggcagacca gctctggcgacggctgcaggagttgctggcccacacg agctcctgggaggaggagctagcagagttgaggcggg agaaa

[0080] TABLE 14 Predicted Amino Acid Sequence of PN13730 MASTNAESQLQRIIRDLQDAVTELSKEFQEAGEPITD (SEQ ID NO:4) DSTSLHKFSYKLEYLLQFDQKEKATLLGNKKDYWDYF CACLAKVKGANDGIRFVKSISELRTSLGKGRAFIRYS LVHQRLADTLQQCFMNTKVTSDWYYARSPFLQPKLSS DIVGQLYELTEVQFDLASRGFDLDAAWPTFARRTLTT GSSAYLWKPPSRSSSMSSLVSSYLQTQEMVSNFDLNS PLNNEALEGFDEMRLELDQLEVREKQLRERMQQLDRE NQELRAAVSQQGEQLQTERERGRTAAEDNVRLTCLVA ELQKQWEVTQATQNTVKELQTCLQGLELGAAEKEEDY HTALRRLESMLQPLAQELEATRDSLDKKNQHLASFPG WLAMAQQKADTASDTKGRQEPIPSDAAQEMQELGEKL QALERERTKVEEVNRQQSAQLEQLVKELQLKEDARAS LERLVKEMAPLQEELSGKGQEADQLWRRLQELLAHTS SWEEELAELRREK

Examples 4-13 Identification of Protein-Protein Interactions

[0081] A yeast two-hybrid system as described in Example 1 using amino acids of the bait as set forth in Table 15 was performed. The clone that was identified by this procedure for each bait is set forth in Table 15 as the prey. The “AA” refers to the amino acids of the bait or prey. The “NUC” refers to the nucleotides of the bait or prey. The Accession numbers refer to GB: GenBank accession numbers. TABLE 15 Ex. BAIT ACCESSION COORDINATES PREY ACCESSION COORDINATES  4 IKKb GB: AF031416 AA: 301-602 EIF3S10 GB: D50929 AA 666-852  5 IKKb GB: AF031416 AA 301-602 SLAP2 GB: AF100750 AA 16-258  6 IKKb GB: AF031416 AA 301-602 KIAA0614 GB: AB014514 AA 549-874  7 IKKb GB: AF031416 AA 301-602 SART-1 GB:AB006198 AA 248-419  8 IKKb GB: AF031416 AA 301-602 GBDR1 GB: NM_006318 AA 4-114  9 IKKa GB: AF009225 AA 599-638 GBDR1 GB: NM_006318 AA 4-114 10 IKKg GB: AF074382 AA 150-302 I-TRAF GB: U59683 AA 17-424 11 IKK-i GB: D63485 AA 450-717 I-TRAF GB: U59683 AA 17-424 12 IKK-i GB: D63485 AA 450-717 NUMA1 GB: Z11583 AA962-1092 13 IKK-i GB: D63485 AA 450-717 SPA-1 GB: AB005666 AA 925-1042

Example 14 Generation of Polyclonal Antibody Against Protein Complexes

[0082] As shown above, IKKb interacts with LDHM to form a complex. A complex of the two proteins is prepared, e.g., by mixing purified preparations of each of the two proteins. If desired, the protein complex can be stabilized by cross-linking the proteins in the complex, by methods known to those of skill in the art. The protein complex is used to immunize rabbits and mice using a procedure similar to that described by Harlow et al. (1988). This procedure has been shown to generate Abs against various other proteins (for example, see Kraemer et al., 1993).

[0083] Briefly, purified protein complex is used as immunogen in rabbits. Rabbits are immunized with 100 μg of the protein in complete Freund's adjuvant and boosted twice in three-week intervals, first with 100 μg of immunogen in incomplete Freund's adjuvant, and followed by 100 μg of immunogen in PBS. Antibody-containing serum is collected two weeks thereafter. The antisera is preadsorbed with IKKb and LDHM, such that the remaining antisera comprises antibodies which bind conformational epitopes, i.e., complex-specific epitopes, present on the IKKb-LDHM complex but not on the monomers.

[0084] Polyclonal antibodies against each of the complexes set forth in Tables 1-12 are prepared in a similar manner by mixing the specified proteins together, immunizing an animal and isolating antibodies specific for the protein complex, but not for the individual proteins.

[0085] Polyclonal antibodies against the protein set forth in Table 14 are prepared in a similar manner by immunizing an animal with the protein and isolating antibodies specific for the protein.

Example 15 Generation of Monoclonal Antibodies Specific for Protein Complexes

[0086] Monoclonal antibodies are generated according to the following protocol. Mice are immunized with immunogen comprising IKKb/LDHM complexes conjugated to keyhole limpet hemocyanin using glutaraldehyde or EDC as is well known in the art. The complexes can be prepared as described in Example 14, and may also be stabilized by cross-linking. The immunogen is mixed with an adjuvant. Each mouse receives four injections of 10 to 100 μg of immunogen, and after the fourth injection blood samples are taken from the mice to determine if the serum contains antibody to the immunogen. Serum titer is determined by ELISA or RIA. Mice with sera indicating the presence of antibody to the immunogen are selected for hybridoma production.

[0087] Spleens are removed from immune mice and a single-cell suspension is prepared (Harlow et al., 1988). Cell fusions are performed essentially as described by Kohler et al. (1975). Briefly, P3.65.3 myeloma cells (American Type Culture Collection, Rockville, Md.) or NS-1 myeloma cells are fused with immune spleen cells using polyethylene glycol as described by Harlow et al. (1988). Cells are plated at a density of 2×10⁵ cells/well in 96-well tissue culture plates. Individual wells are examined for growth, and the supernatants of wells with growth are tested for the presence of IKKb/LDHM complex-specific antibodies by ELISA or RIA using IKKb/LDHM complex as target protein. Cells in positive wells are expanded and subcloned to establish and confirm monoclonality.

[0088] Clones with the desired specificities are expanded and grown as ascites in mice or in a hollow fiber system to produce sufficient quantities of antibodies for characterization and assay development. Antibodies are tested for binding to IKKb alone or to LDHM alone, to determine which are specific for the IKKb/LDHM complex as opposed to those that bind to the individual proteins.

[0089] Monoclonal antibodies against each of the complexes set forth in Tables 1-12 are prepared in a similar manner by mixing the specified proteins together, immunizing an animal, fusing spleen cells with myeloma cells and isolating clones which produce antibodies specific for the protein complex, but not for the individual proteins.

[0090] Monoclonal antibodies against the protein set forth in Table 14 are prepared in a similar manner by immunizing an animal with the protein, fusing spleen cells with myeloma cells and isolating clones which produce antibodies specific for the protein.

Example 16 In vitro Identification of Modulators for Protein-Protein Interactions

[0091] The present invention is useful in screening for agents that modulate the interaction of IKKb and LDHM. The knowledge that IKKb and LDHM form a complex is useful in designing such assays. Candidate agents are screened by mixing IKKb and LDHM (a) in the presence of a candidate agent, and (b) in the absence of the candidate agent. The amount of complex formed is measured for each sample. An agent modulates the interaction of IKKb and LDHM if the amount of complex formed in the presence of the agent is greater than (promoting the interaction), or less than (inhibiting the interaction) the amount of complex formed in the absence of the agent. The amount of complex is measured by a binding assay, which shows the formation of the complex, or by using antibodies immunoreactive to the complex.

[0092] Briefly, a binding assay is performed in which immobilized IKKb is used to bind labeled LDHM. The labeled LDHM is contacted with the immobilized IKKb under aqueous conditions that permit specific binding of the two proteins to form a IKKb/LDHM complex in the absence of an added test agent. Particular aqueous conditions may be selected according to conventional methods. Any reaction condition can be used as long as specific binding of IKKb/LDHM occurs in the control reaction. A parallel binding assay is performed in which the test agent is added to the reaction mixture. The amount of labeled LDHM bound to the immobilized IKKb is determined for the reactions in the absence or presence of the test agent. If the amount of bound, labeled LDHM in the presence of the test agent is different than the amount of bound labeled LDHM in the absence of the test agent, the test agent is a modulator of the interaction of IKKb and LDHM.

[0093] Candidate agents for modulating the interaction of each of the protein complexes set t forth in Tables 1-12 are screened in vitro in a similar manner.

Example 17 In vivo Identification of Modulators for Protein-Protein Interactions

[0094] In addition to the in vitro method described in Example 16, an in vivo assay can also be used to screen for agents which modulate the interaction of IKKb and LDHM. Briefly, a yeast two-hybrid system is used in which the yeast cells express (1) a first fusion protein comprising IKKb or a fragment thereof and a first transcriptional regulatory protein sequence, e.g., GAL4 activation domain, (2) a second fusion protein comprising LDHM or a fragment thereof and a second transcriptional regulatory protein sequence, e.g., GAL4 DNA-binding domain, and (3) a reporter gene, e.g., β-galactosidase, which is transcribed when an intermolecular complex comprising the first fusion protein and the second fusion protein is formed. Parallel reactions are performed in the absence of a test agent as the control and in the presence of the test agent. A functional IKKb/LDHM complex is detected by detecting the amount of reporter gene expressed. If the amount of reporter gene expression in the presence of the test agent is different than the amount of reporter gene expression in the absence of the test agent, the test agent is a modulator of the interaction of IKKb and LDHM.

[0095] Candidate agents for modulating the interaction of each of the protein complexes set forth in Tables 1-12 are screened in vivo in a similar manner.

[0096] While the invention has been disclosed in this patent application by reference to the details of preferred embodiments of the invention, it is to be understood that the disclosure is intended in an illustrative rather than in a limiting sense, as it is contemplated that modifications will readily occur to those skilled in the art, within the spirit of the invention and the scope of the appended claims.

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[0128] PCT Published Application No. WO 97/27296

[0129] PCT Published Application No. WO 99/65939

[0130] U.S. Pat. No. 5,622,852

[0131] U.S. Pat. No. 5,773,218

1 4 1 40 DNA Artificial Sequence oligonucleotide primer 1 gcaggaaaca gctatgacca tacagtcagc ggccgccacc 40 2 39 DNA Artificial Sequence oligonucleotide primer 2 acggccagtc gcgtggagtg ttatgtcatg cggccgcta 39 3 1633 DNA Homo sapiens CDS (152)..(1633) 3 gaaagtttcg gttctgcccg gcggtggacc cacgagcgcg tgccaccatg gagtctgacc 60 actgctgagc agacagccac cgagggccga aattctgagc cttcctctgg acccaggcag 120 gagacataca gacaagaaag gcaaactcac c atg gcc tcc acc aat gca gag 172 Met Ala Ser Thr Asn Ala Glu 1 5 agc cag ctc cag aga atc atc cga gac ttg caa gat gct gtg aca gaa 220 Ser Gln Leu Gln Arg Ile Ile Arg Asp Leu Gln Asp Ala Val Thr Glu 10 15 20 cta agc aaa gaa ttt cag gaa gca ggg gaa ccc atc acg gat gac agc 268 Leu Ser Lys Glu Phe Gln Glu Ala Gly Glu Pro Ile Thr Asp Asp Ser 25 30 35 acc agc ttg cat aaa ttt tct tat aaa ctt gag tat ctc ctg caa ttt 316 Thr Ser Leu His Lys Phe Ser Tyr Lys Leu Glu Tyr Leu Leu Gln Phe 40 45 50 55 gat cag aaa gag aag gcc acc ctc ctg ggc aac aag aag gac tac tgg 364 Asp Gln Lys Glu Lys Ala Thr Leu Leu Gly Asn Lys Lys Asp Tyr Trp 60 65 70 gat tac ttc tgt gcc tgc ctg gcc aag gtg aaa gga gcc aat gat ggg 412 Asp Tyr Phe Cys Ala Cys Leu Ala Lys Val Lys Gly Ala Asn Asp Gly 75 80 85 atc cgc ttt gtc aag tct atc tca gag ctc cga aca tcc ttg ggg aaa 460 Ile Arg Phe Val Lys Ser Ile Ser Glu Leu Arg Thr Ser Leu Gly Lys 90 95 100 gga aga gca ttt att cgc tac tcc ttg gtg cac cag agg ttg gca gac 508 Gly Arg Ala Phe Ile Arg Tyr Ser Leu Val His Gln Arg Leu Ala Asp 105 110 115 acc tta cag cag tgc ttc atg aac acc aaa gtg acc agt gac tgg tac 556 Thr Leu Gln Gln Cys Phe Met Asn Thr Lys Val Thr Ser Asp Trp Tyr 120 125 130 135 tat gca aga agc ccc ttt ctg cag cca aag ctg agc tcg gac att gtg 604 Tyr Ala Arg Ser Pro Phe Leu Gln Pro Lys Leu Ser Ser Asp Ile Val 140 145 150 ggc caa ctc tat gag ctg act gag gtt cag ttt gac ctg gcg tcg agg 652 Gly Gln Leu Tyr Glu Leu Thr Glu Val Gln Phe Asp Leu Ala Ser Arg 155 160 165 ggc ttt gac ttg gat gct gcc tgg cca aca ttt gcc agg agg acg ctg 700 Gly Phe Asp Leu Asp Ala Ala Trp Pro Thr Phe Ala Arg Arg Thr Leu 170 175 180 acc act ggc tct tct gct tac ctg tgg aaa ccc cct agc cgc agc tcc 748 Thr Thr Gly Ser Ser Ala Tyr Leu Trp Lys Pro Pro Ser Arg Ser Ser 185 190 195 agc atg agc agc ttg gtg agc agc tac ctg cag act caa gag atg gtg 796 Ser Met Ser Ser Leu Val Ser Ser Tyr Leu Gln Thr Gln Glu Met Val 200 205 210 215 tcc aac ttt gac ctg aac agc ccc cta aac aac gag gca ttg gag ggc 844 Ser Asn Phe Asp Leu Asn Ser Pro Leu Asn Asn Glu Ala Leu Glu Gly 220 225 230 ttt gat gag atg cga cta gag ctg gac cag ttg gag gtg cgg gag aag 892 Phe Asp Glu Met Arg Leu Glu Leu Asp Gln Leu Glu Val Arg Glu Lys 235 240 245 cag cta cgg gag cgc atg cag cag ctg gac aga gag aac cag gag ctg 940 Gln Leu Arg Glu Arg Met Gln Gln Leu Asp Arg Glu Asn Gln Glu Leu 250 255 260 agg gca gct gtc agc cag caa ggg gag caa ctg cag aca gag agg gag 988 Arg Ala Ala Val Ser Gln Gln Gly Glu Gln Leu Gln Thr Glu Arg Glu 265 270 275 agg ggg cgc act gca gcg gag gac aac gtt cgc ctc act tgc ttg gta 1036 Arg Gly Arg Thr Ala Ala Glu Asp Asn Val Arg Leu Thr Cys Leu Val 280 285 290 295 gct gag ctc cag aag cag tgg gag gtc acc cag gcc acc cag aac act 1084 Ala Glu Leu Gln Lys Gln Trp Glu Val Thr Gln Ala Thr Gln Asn Thr 300 305 310 gtg aag gag ctg cag aca tgc ctg cag ggc ctg gag cta gga gca gca 1132 Val Lys Glu Leu Gln Thr Cys Leu Gln Gly Leu Glu Leu Gly Ala Ala 315 320 325 gag aag gag gag gac tac cac aca gcc ctg cgg cgg ctg gag tcc atg 1180 Glu Lys Glu Glu Asp Tyr His Thr Ala Leu Arg Arg Leu Glu Ser Met 330 335 340 ctg cag ccc ttg gca cag gag ctt gag gcc aca cgg gac tca ctg gac 1228 Leu Gln Pro Leu Ala Gln Glu Leu Glu Ala Thr Arg Asp Ser Leu Asp 345 350 355 aag aaa aac cag cat tta gcc agc ttc cca ggc tgg cta gcc atg gct 1276 Lys Lys Asn Gln His Leu Ala Ser Phe Pro Gly Trp Leu Ala Met Ala 360 365 370 375 cag cag aag gca gat acg gca tca gac aca aag ggc cgg caa gaa cct 1324 Gln Gln Lys Ala Asp Thr Ala Ser Asp Thr Lys Gly Arg Gln Glu Pro 380 385 390 att ccc agt gat gcg gcc cag gag atg cag gag cta ggg gag aag ctt 1372 Ile Pro Ser Asp Ala Ala Gln Glu Met Gln Glu Leu Gly Glu Lys Leu 395 400 405 caa gcc cta gaa agg gag aga acc aag gtc gag gag gtc aac aga cag 1420 Gln Ala Leu Glu Arg Glu Arg Thr Lys Val Glu Glu Val Asn Arg Gln 410 415 420 cag agt gcc caa ctg gaa cag ctg gtc aag gag ctt cag ctg aaa gag 1468 Gln Ser Ala Gln Leu Glu Gln Leu Val Lys Glu Leu Gln Leu Lys Glu 425 430 435 gat gcc cgg gcc agc ctg gag cgc ctg gtg aag gag atg gcc cca ctc 1516 Asp Ala Arg Ala Ser Leu Glu Arg Leu Val Lys Glu Met Ala Pro Leu 440 445 450 455 cag gag gag ttg tct ggg aag gga cag gag gca gac cag ctc tgg cga 1564 Gln Glu Glu Leu Ser Gly Lys Gly Gln Glu Ala Asp Gln Leu Trp Arg 460 465 470 cgg ctg cag gag ttg ctg gcc cac acg agc tcc tgg gag gag gag cta 1612 Arg Leu Gln Glu Leu Leu Ala His Thr Ser Ser Trp Glu Glu Glu Leu 475 480 485 gca gag ttg agg cgg gag aaa 1633 Ala Glu Leu Arg Arg Glu Lys 490 4 494 PRT Homo sapiens 4 Met Ala Ser Thr Asn Ala Glu Ser Gln Leu Gln Arg Ile Ile Arg Asp 1 5 10 15 Leu Gln Asp Ala Val Thr Glu Leu Ser Lys Glu Phe Gln Glu Ala Gly 20 25 30 Glu Pro Ile Thr Asp Asp Ser Thr Ser Leu His Lys Phe Ser Tyr Lys 35 40 45 Leu Glu Tyr Leu Leu Gln Phe Asp Gln Lys Glu Lys Ala Thr Leu Leu 50 55 60 Gly Asn Lys Lys Asp Tyr Trp Asp Tyr Phe Cys Ala Cys Leu Ala Lys 65 70 75 80 Val Lys Gly Ala Asn Asp Gly Ile Arg Phe Val Lys Ser Ile Ser Glu 85 90 95 Leu Arg Thr Ser Leu Gly Lys Gly Arg Ala Phe Ile Arg Tyr Ser Leu 100 105 110 Val His Gln Arg Leu Ala Asp Thr Leu Gln Gln Cys Phe Met Asn Thr 115 120 125 Lys Val Thr Ser Asp Trp Tyr Tyr Ala Arg Ser Pro Phe Leu Gln Pro 130 135 140 Lys Leu Ser Ser Asp Ile Val Gly Gln Leu Tyr Glu Leu Thr Glu Val 145 150 155 160 Gln Phe Asp Leu Ala Ser Arg Gly Phe Asp Leu Asp Ala Ala Trp Pro 165 170 175 Thr Phe Ala Arg Arg Thr Leu Thr Thr Gly Ser Ser Ala Tyr Leu Trp 180 185 190 Lys Pro Pro Ser Arg Ser Ser Ser Met Ser Ser Leu Val Ser Ser Tyr 195 200 205 Leu Gln Thr Gln Glu Met Val Ser Asn Phe Asp Leu Asn Ser Pro Leu 210 215 220 Asn Asn Glu Ala Leu Glu Gly Phe Asp Glu Met Arg Leu Glu Leu Asp 225 230 235 240 Gln Leu Glu Val Arg Glu Lys Gln Leu Arg Glu Arg Met Gln Gln Leu 245 250 255 Asp Arg Glu Asn Gln Glu Leu Arg Ala Ala Val Ser Gln Gln Gly Glu 260 265 270 Gln Leu Gln Thr Glu Arg Glu Arg Gly Arg Thr Ala Ala Glu Asp Asn 275 280 285 Val Arg Leu Thr Cys Leu Val Ala Glu Leu Gln Lys Gln Trp Glu Val 290 295 300 Thr Gln Ala Thr Gln Asn Thr Val Lys Glu Leu Gln Thr Cys Leu Gln 305 310 315 320 Gly Leu Glu Leu Gly Ala Ala Glu Lys Glu Glu Asp Tyr His Thr Ala 325 330 335 Leu Arg Arg Leu Glu Ser Met Leu Gln Pro Leu Ala Gln Glu Leu Glu 340 345 350 Ala Thr Arg Asp Ser Leu Asp Lys Lys Asn Gln His Leu Ala Ser Phe 355 360 365 Pro Gly Trp Leu Ala Met Ala Gln Gln Lys Ala Asp Thr Ala Ser Asp 370 375 380 Thr Lys Gly Arg Gln Glu Pro Ile Pro Ser Asp Ala Ala Gln Glu Met 385 390 395 400 Gln Glu Leu Gly Glu Lys Leu Gln Ala Leu Glu Arg Glu Arg Thr Lys 405 410 415 Val Glu Glu Val Asn Arg Gln Gln Ser Ala Gln Leu Glu Gln Leu Val 420 425 430 Lys Glu Leu Gln Leu Lys Glu Asp Ala Arg Ala Ser Leu Glu Arg Leu 435 440 445 Val Lys Glu Met Ala Pro Leu Gln Glu Glu Leu Ser Gly Lys Gly Gln 450 455 460 Glu Ala Asp Gln Leu Trp Arg Arg Leu Gln Glu Leu Leu Ala His Thr 465 470 475 480 Ser Ser Trp Glu Glu Glu Leu Ala Glu Leu Arg Arg Glu Lys 485 490 

What is claimed is:
 1. An isolated protein complex comprising two proteins, the protein complex selected from the group consisting of: (i) a complex of a first protein and a second protein; (ii) a complex of a fragment of said first protein and said second protein; (iii) a complex of said first protein and a fragment of said second protein; and (iv) a complex of a fragment of said first protein and a fragment of said second protein, wherein said first and second proteins are selected from the group consisting of: (a) said first protein is IKKb and said second protein is selected from the group consisting of LDHM, EIF3S10, SLAP2, KIAA0614, SART-1 and GBDR1; (b) said first protein is IKKa and said second protein is GBDR1; (c) said first protein is IKKg and said second protein is TRAF; and (d) said first protein is IKK-i and said second protein is selected from the group consisting of NUMA1, SPA-1 and PN13730.
 2. The protein complex of claim 1, wherein said protein complex comprises said first protein and said second protein.
 3. The protein complex of claim 1, wherein said protein complex comprises a fragment of said first protein and said second protein or said first protein and a fragment of said second protein.
 4. The protein complex of claim 1, wherein said protein complex comprises fragments of said first protein and said second protein.
 5. An isolated antibody selectively immunoreactive with a protein complex of claim
 1. 6. The antibody of claim 5, wherein said antibody is a monoclonal antibody.
 7. A method for diagnosing a physiological disorder in an animal, which comprises assaying for: (a) whether a protein complex set forth in claim 1 is present in a tissue extract; (b) the ability of proteins to form a protein complex set forth in claim 1; and (c) a mutation in a gene encoding a protein of a protein complex set forth in claim
 1. 8. The method of claim 7, wherein said animal is a human.
 9. The method of claim 8, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 10. The method of claim 7, wherein the diagnosis is for a predisposition to said physiological disorder.
 11. The method of claim 7, wherein the diagnosis is for the existence of said physiological disorder.
 12. The method of claim 7, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 13. The method of claim 7, wherein said assay comprises a yeast two-hybrid assay.
 14. The method of claim 7, wherein said assay comprises measuring in vitro a complex formed by combining the proteins of the protein complex, said proteins isolated from said animal.
 15. The method of claim 14, wherein said complex is measured by binding with an antibody specific for said complex.
 16. The method of claim 7, wherein said assay comprises mixing an antibody specific for said protein complex with a tissue extract from said animal and measuring the binding of said antibody.
 17. A method for determining whether a mutation in a gene encoding one of the proteins of a protein complex set forth in claim 1 is useful for diagnosing a physiological disorder, which comprises assaying for the ability of said protein with said mutation to form a complex with the other protein of said protein complex, wherein an inability to form said complex is indicative of said mutation being useful for diagnosing a physiological disorder.
 18. The method of claim 17, wherein said gene is an animal gene.
 19. The method of claim 18, wherein said animal is a human.
 20. The method of claim 19, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 21. The method of claim 17, wherein the diagnosis is for a predisposition to a physiological disorder.
 22. The method of claim 17, wherein the diagnosis is for the existence of a physiological disorder.
 23. The method of claim 17, wherein said assay comprises a yeast two-hybrid assay.
 24. The method of claim 17, wherein said assay comprises measuring in vitro a complex formed by combining the proteins of the protein complex, said proteins isolated from an animal.
 25. The method of claim 24, wherein said animal is a human.
 26. The method of claim 24, wherein said complex is measured by binding with an antibody specific for said complex.
 27. A non-human animal model for a physiological disorder wherein the genome of said animal or an ancestor thereof has been modified such that the formation of a protein complex set forth in claim 1 has been altered.
 28. The non-human animal model of claim 27, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 29. The non-human animal model of claim 27, wherein the formation of said protein complex has been altered as a result of: (a) over-expression of at least one of the proteins of said protein complex; (b) replacement of a gene for at least one of the proteins of said protein complex with a gene from a second animal and expression of said protein; (c) expression of a mutant form of at least one of the proteins of said protein complex; (d) a lack of expression of at least one of the proteins of said protein complex; or (e) reduced expression of at least one of the proteins of said protein complex.
 30. A cell line obtained from the animal model of claim
 27. 31. A non-human animal model for a physiological disorder, wherein the biological activity of a protein complex set forth in claim 1 has been altered.
 32. The non-human animal model of claim 31, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 33. The non-human animal model of claim 31, wherein said biological activity has been altered as a result of: (a) disrupting the formation of said complex; or (b) disrupting the action of said complex.
 34. The non-human animal model of claim 31, wherein the formation of said complex is disrupted by binding an antibody to at least one of the proteins which form said protein complex.
 35. The non-human animal model of claim 31, wherein the action of said complex is disrupted by binding an antibody to said complex.
 36. The non-human animal model of claim 31, wherein the formation of said complex is disrupted by binding a small molecule to at least one of the proteins which form said protein complex.
 37. The non-human animal model of claim 31, wherein the action of said complex is disrupted by binding a small molecule to said complex.
 38. A cell in which the genome of cells of said cell line has been modified to produce at least one protein complex set forth in claim
 1. 39. A cell line in which the genome of the cells of said cell line has been modified to eliminate at least one protein of a protein complex set forth in claim
 1. 40. A composition comprising: a first expression vector having a nucleic acid encoding a first protein or a homologue or derivative or fragment thereof; and a second expression vector having a nucleic acid encoding a second protein, or a homologue or derivative or fragment thereof, wherein said first and said second proteins are the proteins of claim
 1. 41. A host cell comprising: a first expression vector having a nucleic acid encoding a first protein which is first protein or a homologue or derivative or fragment thereof; and a second expression vector having a nucleic acid encoding a second protein which is second protein, or a homologue or derivative or fragment thereof thereof, wherein said first and said second proteins are the proteins of claim
 1. 42. The host cell of claim 41, wherein said host cell is a yeast cell.
 43. The host cell of claim 41, wherein said first and second proteins are expressed in fusion proteins.
 44. The host cell of claim 41, wherein one of said first and second nucleic acids is linked to a nucleic acid encoding a DNA binding domain, and the other of said first and second nucleic acids is linked to a nucleic acid encoding a transcription-activation domain, whereby two fusion proteins can be produced in said host cell.
 45. The host cell of claim 41, further comprising a reporter gene, wherein the expression of the reporter gene is determined by the interaction between the first protein and the second protein.
 46. A method for screening for drug candidates capable of modulating the interaction of the proteins of a protein complex, the protein complex selected from the group consisting of the protein complexes of claim 1, said method comprising (i) combining the proteins of said protein complex in the presence of a drug to form a first complex; (ii) combining the proteins in the absence of said drug to form a second complex; (iii) measuring the amount of said first complex and said second complex; and (iv) comparing the amount of said first complex with the amount of said second complex, wherein if the amount of said first complex is greater than, or less than the amount of said second complex, then the drug is a drug candidate for modulating the interaction of the proteins of said protein complex.
 47. The method of claim 46, wherein said screening is an in vitro screening.
 48. The method of claim 46, wherein said complex is measured by binding with an antibody specific for said protein complexes.
 49. The method of claim 46, wherein if the amount of said first complex is greater than the amount of said second complex, then said drug is a drug candidate for promoting the interaction of said proteins.
 50. The method of claim 46, wherein if the amount of said first complex is less than the amount of said second complex, then said drug is a drug candidate for inhibiting the interaction of said proteins.
 51. A drug useful for treating a physiological disorder identified by the method of claim
 46. 52. The drug of claim 51, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 53. A method of screening for drug candidates useful in treating a physiological disorder which comprises the steps of: (a) measuring the activity of a protein selected from the group consisting of a first protein and a second protein in the presence of a drug, wherein said first and second proteins are selected from the group consisting of the proteins of claim 1, (b) measuring the activity of said protein in the absence of said drug, and (c) comparing the activity measured in steps (1) and (2), wherein if there is a difference in activity, then said drug is a drug candidate for treating said physiological disorder.
 54. A drug useful for treating a physiological disorder identified by the method of claim
 53. 55. The drug of claim 54, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 56. A method for selecting modulators of a protein complex formed between a first protein or a homologue or derivative or fragment thereof and a second protein or a homologue or derivative or fragment thereof, wherein said first and second proteins are selected from the group consisting of the proteins of claim 1, said method comprising: providing the protein complex; contacting said protein complex with a test compound; and determining the presence or absence of binding of said test compound to said protein complex.
 57. A modulator useful for treating a physiological disorder identified by the method of claim
 56. 58. The modulator of claim 57, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 59. A method for selecting modulators of an interaction between a first protein and a second protein, said first protein or a homologue or derivative or fragment thereof and said second protein or a homologue or derivative or fragment thereof, wherein said first and second proteins are selected from the group consisting of the proteins of claim 1, said method comprising: contacting said first protein with said second protein in the presence of a test compound; and determining the interaction between said first protein and said second protein.
 60. The method of claim 59, wherein at least one of said first and second proteins is a fusion protein having a detectable tag.
 61. The method of claim 59, wherein said step of determining the interaction between said first protein and said second protein is conducted in a substantially cell free environment.
 62. The method of claim 59, wherein the interaction between said first protein and said second protein is determined in a host cell.
 63. The method of claim 62, wherein said host cell is a yeast cell.
 64. The method of claim 59, wherein said test compound is provided in a phage display library.
 65. The method of claim 59, wherein said test compound is provided in a combinatorial library.
 66. A modulator useful for treating a physiological disorder identified by the method of claim
 59. 67. The modulator of claim 66, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 68. A method for selecting modulators of a protein complex formed from a first protein or a homologue or derivative or fragment thereof, and a second protein or a homologue or derivative or fragment thereof, wherein said first and second proteins are selected from the group consisting of the proteins of claim 1, said method comprising: contacting said protein complex with a test compound; and determining the interaction between said first protein and said second protein.
 69. A modulator useful for treating a physiological disorder identified by the method of claim
 68. 70. The modulator of claim 69, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 71. A method for selecting modulators of an interaction between a first polypeptide and a second polypeptide, said first polypeptide being a first protein or a homologue or derivative or fragment thereof and said second polypeptide being a second protein or a homologue or derivative or fragment thereof, wherein said first and second proteins are selected from the group consisting of the proteins of claim 1, said method comprising: providing in a host cell a first fusion protein having said first polypeptide, and a second fusion protein having said second polypeptide, wherein a DNA binding domain is fused to one of said first and second polypeptides while a transcription-activating domain is fused to the other of said first and second polypeptides; providing in said host cell a reporter gene, wherein the transcription of the reporter gene is determined by the interaction between the first polypeptide and the second polypeptide; allowing said first and second fusion proteins to interact with each other within said host cell in the presence of a test compound; and determining the presence or absence of expression of said reporter gene.
 72. The method of claim 71, wherein said host cell is a yeast cell.
 73. A modulator useful for treating a physiological disorder identified by the method of claim
 71. 74. The modulator of claim 73, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 75. A method for identifying a compound that binds to a protein in vitro, wherein said protein is selected from the group consisting of the proteins of claim 1, said method comprising: contacting a test compound with said protein for a time sufficient to form a complex and detecting for the formation of a complex by detecting said protein or the compound in the complex, so that if a complex is detected, a compound that binds to protein is identified.
 76. A compound useful for treating a physiological disorder identified by the method of claim
 75. 77. The compound of claim 76, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 78. A method for selecting modulators of an interaction between a first polypeptide and a second polypeptide, said first polypeptide being a first protein or a homologue or derivative or fragment thereof and said second polypeptide being a second protein or a homologue or derivative or fragment thereof, wherein said first and second proteins are selected from the group consisting of the proteins of claim 1, said method comprising: providing atomic coordinates defining a three-dimensional structure of a protein complex formed by said first polypeptide and said second polypeptide; and designing or selecting compounds capable of modulating the interaction between a first polypeptide and a second polypeptide based on said atomic coordinates.
 79. A modulator useful for treating a physiological disorder identified by the method of claim
 78. 80. The modulator of claim 79, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 81. A method for providing inhibitors of an interaction between a first polypeptide and a second polypeptide, said first polypeptide being a first protein or a homologue or derivative or fragment thereof and said second polypeptide being a second protein or a homologue or derivative or fragment thereof, wherein said first and second proteins are selected from the group consisting of the proteins of claim 1, said method comprising: providing atomic coordinates defining a three-dimensional structure of a protein complex formed by said first polypeptide and said second polypeptide; and designing or selecting compounds capable of interfering with the interaction between a first polypeptide and a second polypeptide based on said atomic coordinates.
 82. An inhibitor useful for treating a physiological disorder identified by the method of claim
 81. 83. The inhibitor of claim 82, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 84. A method for selecting modulators of a protein, wherein said protein is selected from the group consisting of the proteins of claim 1, said method comprising: contacting said protein with a test compound; and determining binding of said test compound to said protein.
 85. The method of claim 84, wherein said test compound is provided in a phage display library.
 86. The method of claim 84, wherein said test compound is provided in a combinatorial library.
 87. A modulator useful for treating a physiological disorder identified by the method of claim
 84. 88. The modulator of claim 87, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 89. A method for modulating, in a cell, a protein complex having a first protein interacting with a second protein, wherein said first and second proteins are selected from the group consisting of the proteins of claim 1, said method comprising: administering to said cell a compound capable of modulating said protein complex.
 90. The method of claim 89, wherein said compound is selected from the group consisting of: (a) a compound which is capable of interfering with the interaction between said first protein and said second protein, (b) a compound which is capable of binding at least one of said first protein and said A second protein, (c) a compound which comprises a peptide having a contiguous span of amino acids of at least 4 amino acids of said second protein and capable of binding said first protein, (d) a compound which comprises a peptide capable of binding said first protein and having an amino acid sequence of from 4 to 30 amino acids that is at least 75% identical to a contiguous span of amino acids of said second protein of the same length, (e) a compound which comprises a peptide having a contiguous span of amino acids of at least 4 amino acids of said first protein and capable of binding said second protein, (f) a compound which comprises a peptide capable of binding said second protein and having an amino acid sequence of from 4 to 30 amino acids that is at least 75% identical to a contiguous span of amino acids of said first protein of the same length, (g) a compound which is an antibody immunoreactive with said first protein or said second protein, (h) a compound which is a nucleic acid encoding an antibody immunoreactive with said first protein or said second protein, (i) a compound which modulates the expression of said first protein or said second protein, (j) a compound which is an antisense compound or a ribozyme specifically hybridizing to a nucleic acid encoding said first protein or complement thereof, and (k) a compound which is an antisense compound or a ribozyme specifically hybridizing to a nucleic acid encoding said second protein or complement thereof.
 91. A method for modulating, in a cell, a protein complex having a first protein interacting with a second protein, wherein said first and second proteins are selected from the group consisting of the proteins of claim 1, said method comprising: administering to said cell a peptide capable of interfering with the interaction between said first protein and said second protein, wherein said peptide is associated with a transporter capable of increasing cellular uptake of said peptide.
 92. The method of claim 91, wherein said peptide is covalently linked to said transporter which is selected from the group consisting of penetratins, l-Tat₄₉₋₅₇, d-Tat₄₉₋₅₇, retro-inverso isomers of l- or d-Tat₄₉₋₅₇, L-arginine oligomers, D-arginine oligomers, L-lysine oligomers, D-lysine oligomers, L-histine oligomers, D-histine oligomers, L-ornithine oligomers, D-ornithine oligomers, short peptide sequences derived from fibroblast growth factor, Galparan, and HSV-1 structural protein VP22, and peptoid analogs thereof.
 93. A method for modulating, in a cell, the interaction of a protein with a ligand, wherein said protein is selected from the group consisting of the first or second proteins of claim 1, said method comprising: administering to said cell a compound capable of modulating said interaction.
 94. The method of claim 93, wherein said protein is one of said first or second proteins and said ligand is the other of said first or second proteins
 95. The method of claim 93, wherein said compound is selected from the group consisting of: (a) a compound which interferes with said interaction, (b) a compound which binds to said protein or said ligand, (c) a compound which comprises a peptide having a contiguous span of amino acids of at least 4 amino acids of said protein and capable of binding said ligand, (d) a compound which comprises a peptide capable of binding said ligand and having an amino acid sequence of from 4 to 30 amino acids that is at least 75% identical to a contiguous span of amino acids of said protein of the same length, (e) a compound which is an antibody immunoreactive with said protein or said ligand, (f) a compound which is a nucleic acid encoding an antibody immunoreactive with said ligand or said protein, (g) a compound which modulates the expression of said protein or said ligand, and (h) a compound which is an antisense compound or a ribozyme specifically hybridizing to a nucleic acid encoding said ligand or said protein or complement thereof.
 96. A method for modulating neuronal death in a patient having a physiological disorder comprising: modulating a protein complex having a first protein interacting with a second to protein, wherein said first and second proteins are selected from the group consisting of the proteins of claim
 1. 97. The method of claim 96, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 98. A method for modulating neuronal death in a patient having physiological disorder comprising: administering to the patient a compound capable of modulating a protein complex having a first protein interacting with a second protein, wherein said first and second proteins are selected from the group consisting of the proteins of claim
 1. 99. The method of claim 98, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 100. The method of claim 98, wherein said compound is selected from the group consisting of: (a) a compound which is capable of interfering with the interaction between said first protein and said second protein, (b) a compound which is capable of binding at least one of said first protein and said second protein, (c) a compound which comprises a peptide having a contiguous span of amino acids of at least 4 amino acids of a second protein and capable of binding a first protein, (d) a compound which comprises a peptide capable of binding a first protein and having an amino acid sequence of from 4 to 30 amino acids that is at least 75% identical to a contiguous span of amino acids of a second protein of the same length, (e) a compound which comprises a peptide having a contiguous span of amino acids of at least 4 amino acids of first protein and capable of binding a second protein, (f) a compound which comprises a peptide capable of binding a second protein and having an amino acid sequence of from 4 to 30 amino acids that is at least 75% identical to to a contiguous span of amino acids of a first protein of the same length, (g) a compound which is an antibody immunoreactive with a first protein or a second protein, (h) a compound which is a nucleic acid encoding an antibody immunoreactive with a first protein or a second protein, (i) a compound which modulates the expression of a first protein or a second protein, (j) a compound which is an antisense compound or a ribozyme specifically hybridizing to a nucleic acid encoding a first protein or complement thereof, and (j) a compound which is an antisense compound or a ribozyme specifically hybridizing to a nucleic acid encoding a second protein or complement thereof
 101. A method for modulating neuronal death in a patient having physiological disorder comprising: administering to said cell a peptide capable of interfering with the interaction between a first protein and a second protein, wherein said first and second proteins are selected from the group consisting of the proteins of claim 1, wherein said peptide is associated with a transporter capable of increasing cellular uptake of said peptide.
 102. The method of claim 101, wherein said peptide is covalently linked to said transporter which is selected from the group consisting of penetratins, l-Tat₄₉₋₅₇, d-Tat₄₉₋₅₇, retro-inverso isomers of l- or d-Tat₄₉₋₅₇, L-arginine oligomers, D-arginine oligomers, L-lysine oligomers, D-lysine oligomers, L-histine oligomers, D-histine oligomers, L-ornithine oligomers, D-ornithine oligomers, short peptide sequences derived from fibroblast growth factor, Galparan, and HSV-1 structural protein VP22, and peptoid analogs thereof.
 103. A method for treating a physiological disorder comprising: administering to a patient in need of treatment a compound capable of modulating a protein complex having a first protein interacting with a second protein, wherein said first and second proteins are selected from the group consisting of the proteins of claim
 1. 104. The method of claim 103, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 105. The method of claim 103, wherein said compound is selected from the group consisting of: (a) a compound which is capable of interfering with the interaction between said first protein and said second protein, (b) a compound which is capable of binding at least one of said first protein and said second protein, (c) a compound which comprises a peptide having a contiguous span of amino acids of at least 4 amino acids of said second protein and capable of binding said first protein, (d) a compound which comprises a peptide capable of binding said first protein and having an amino acid sequence of from 4 to 30 amino acids that is at least 75% identical to a contiguous span of amino acids of said second protein of the same length, (e) a compound which comprises a peptide having a contiguous span of amino acids of at least 4 amino acids of first protein and capable of binding said second protein, (f) a compound which comprises a peptide capable of binding said second protein and having an amino acid sequence of from 4 to 30 amino acids that is at least 75% identical to a contiguous span of amino acids of said first protein of the same length, (g) a compound which is an antibody immunoreactive with said first protein or said second protein, (h) a compound which is a nucleic acid encoding an antibody immunoreactive with said first protein or said second protein, (i) a compound which modulates the expression of said first protein or said second protein, (j) a compound which is an antisense compound or a ribozyme specifically hybridizing to a nucleic acid encoding a first protein or complement thereof, (k) a compound which is an antisense compound or a ribozyme specifically hybridizing to a nucleic acid encoding a second protein or complement thereof, and (l) a compound which is capable of strengthening the interaction between said first protein and said second protein.
 106. A method for treating a physiological disorder comprising: administering to said cell a peptide capable of interfering with the interaction between a first protein and a second protein, wherein said first and second proteins are selected from the group consisting of the proteins of claim 1, wherein said peptide is associated with a transporter capable of increasing cellular uptake of said peptide.
 107. The method of claim 106, wherein said peptide is covalently linked to said transporter which is selected from the group consisting of penetratins, l-Tat₄₉₋₅₇, d-Tat₄₉₋₅₇, retro-inverso isomers of l- or d-Tat₄₉₋₅₇, L-arginine oligomers, D-arginine oligomers, L-lysine oligomers, D-lysine oligomers, L-histine oligomers, D-histine oligomers, L-ornithine oligomers, D-ornithine oligomers, short peptide sequences derived from fibroblast growth factor, Galparan, and HSV-1 structural protein VP22, and peptoid analogs thereof.
 108. The method of claim 106, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 109. A method for treating a physiological disorder comprising: administering to a patient in need of treatment a compound capable of modulating the activity of a first protein or a second protein, wherein said first and second proteins are selected from the group consisting of the proteins of claim
 1. 110. The method of claim 109, wherein said physiological disorder is selected from the group consisting of inflammatory disease, rheumatoid arthritis, osteoarthritis, asthma, arteriosclerosis, inflammatory bowel disease and cancer.
 111. The method of claim 109, wherein the activity is the interaction of said first protein or said second protein with a ligand.
 112. The method of claim 111, wherein said ligand is the other of said first or second protein.
 113. A method of modulating activity in a cell of a protein, said protein being first protein or a second protein selected from the group consisting of the proteins of claim 1, said method comprising: administering to said cell a compound capable of modulating said protein.
 114. The method of claim 113, wherein said compound is selected from the group consisting of: (a) a compound which is capable of binding said protein, (b) a compound which comprises a peptide having a contiguous span of at least 4 amino acids of a first protein and capable of binding a second protein, (c) a compound which comprises a peptide capable of binding a second protein and having an amino acid sequence of from 4 to 30 amino acids that is at least 75% identical to a contiguous span of amino acids of a first protein of the same length, (d) a compound which is an antibody immunoreactive with said protein, (e) a compound which is a nucleic acid encoding an antibody immunoreactive with said protein, and (f) a compound which is an antisense compound or a ribozyme specifically hybridizing to a nucleic acid encoding said protein or complement thereof.
 115. A method for modulating activities of a protein in a cell, said protein being a first protein or a second protein selected from the group consisting of the proteins of claim 1, said method comprising: administering to said cell a peptide having a contiguous span of at least 4 amino acids of one of said first or second proteins and capable of binding the other of said first or second proteins, wherein said peptide is associated with a transporter capable of increasing cellular uptake of said peptide.
 116. The method of claim 115, wherein said peptide is covalently linked to said transporter which is selected from the group consisting of penetratins, l-Tat₄₉₋₅₇, d-Tat₄₉₋₅₇, retro-inverso isomers of l- or d-Tat₄₉₋₅₇, L-arginine oligomers, D-arginine oligomers, L-lysine oligomers, D-lysine oligomers, L-histine oligomers, D-histine oligomers, L-ornithine oligomers, D-ornithine oligomers, short peptide sequences derived from fibroblast growth factor, Galparan, and HSV-1 structural protein VP22, and peptoid analogs thereof.
 117. An isolated nucleic acid encoding a protein comprising an amino acid sequence set forth in SEQ ID NO:4.
 118. The isolated nucleic acid sequence of claim 117 which comprises nucleotides 152-1633 of SEQ ID NO:3 or complement thereof.
 119. An isolated nucleic acid encoding a protein comprising an amino acid sequence which is at least 70% identical to the amino acid sequence set forth in SEQ ID NO:4 and which is capable of interacting with IKK-i.
 120. An isolated nucleic acid comprising a nucleotide sequence which is at least 60% identical to nucleotides 152-1633 of SEQ ID NO:3 or complement thereof.
 121. An isolated nucleic acid sequence comprising a nucleotide sequence set forth in SEQ ID NO:3 or complement thereof.
 122. An isolated nucleic acid comprising a contiguous span of at least 17 nucleotides of the nucleotide sequence set forth in SEQ ID NO:3 or complement thereof.
 123. The isolated nucleic acid of claim 122 comprising at least 21 nucleotides.
 124. The isolated nucleic acid of claim 122 comprising at least 25 nucleotides.
 125. The isolated nucleic acid of claim 122 comprising at least 30 nucleotides.
 126. The isolated nucleic acid of claim 122 comprising at least 50 nucleotides.
 127. An isolated nucleic acid comprising at least 21 nucleotides that encodes a contiguous span of at least 7 amino acids of the amino acid sequence set forth in SEQ ID NO:4.
 128. The isolated nucleic acid of claim 127 encoding at least 8 contiguous amino acids.
 129. The isolated nucleic acid of claim 127 encoding at least 9 contiguous amino acids.
 130. The isolated nucleic acid of claim 127 encoding at least 10 contiguous amino acids.
 131. The isolated nucleic acid of claim 127 encoding at least 15 contiguous amino acids.
 132. The isolated nucleic acid of claim 127 encoding at least 20 contiguous amino acids.
 133. The isolated nucleic acid of claim 127 encoding at least 25 contiguous amino acids.
 134. A nucleic acid vector comprising the isolated nucleic acid of claim
 117. 135. A nucleic acid vector comprising the isolated nucleic acid of claim
 118. 136. A nucleic acid vector comprising the isolated nucleic acid of claim
 119. 137. A nucleic acid vector comprising the isolated nucleic acid of claim
 124. 138. A nucleic acid vector comprising the isolated nucleic acid of claim
 130. 139. A host cell comprising the isolated nucleic acid of claim
 117. 140. A host cell comprising the isolated nucleic acid of claim
 118. 141. A host cell comprising the isolated nucleic acid of claim
 119. 142. A host cell comprising the isolated nucleic acid of claim
 116. 143. A host cell comprising the isolated nucleic acid of claim
 130. 144. A microarray comprising the isolated nucleic acid of claim
 130. 145. An isolated polypeptide comprising an amino acid sequence set forth in SEQ ID NO:4.
 146. An isolated polypeptide comprising an amino acid sequence that is at least 70% identical to the amino acid sequence set forth in SEQ ID NO:4 and capable of interacting with IKK-i.
 147. An isolated polypeptide comprising a contiguous span of at least 8 amino acids of the amino acid sequence set forth in SEQ ID NO:4.
 148. The isolated polypeptide of claim 147 comprising a contiguous span of at least 10 amino acids.
 149. The isolated polypeptide of claim 147 comprising a contiguous span of at least 12 amino acids.
 150. The isolated polypeptide of claim 147 comprising a contiguous span of at least 15 amino acids.
 151. The isolated polypeptide of claim 147 comprising a contiguous span of at least 17 amino acids.
 152. The isolated polypeptide of claim 147 comprising a contiguous span of at least 20 amino acids.
 153. The isolated polypeptide of claim 152 capable of interacting with IKK-i.
 154. An isolated polypeptide comprising an amino acid sequence of from 4 to 30 amino acids that is at least 75% identical to a contiguous span of amino acids of the amino acid sequence set forth in SEQ ID NO:4 of the same length, wherein said isolated polypeptide is capable of interacting with IKK-i.
 155. The isolated polypeptide of claim 154, wherein said amino acid sequence comprises from 8 to 20 amino acids.
 156. An antibody which is specifically immunoreactive with the isolated polypeptide of claim
 145. 157. An antibody which is specifically immunoreactive with the isolated polypeptide of claim
 147. 158. A protein microarray comprising the isolated polypeptide of claim
 145. 159. A protein microarray comprising the isolated polypeptide of claim
 147. 160. A protein microarray comprising the isolated polypeptide of claim
 155. 161. A method for making an isolated polypeptide comprising an amino acid sequence set forth in SEQ ID NO:4, comprising: providing an expression vector comprising a nucleic acid encoding said amino acid sequence; and introducing said expression vector into a host cell such that said host cell producing the isolated polypeptide. 